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Stability indicating HPLC method for the simultaneous determination of dapagliflozin and saxagliptin in bulk and tablet dosage form

机译:同时测定散装和片剂剂型中达格列净和沙格列汀的稳定性指示HPLC方法

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A simple, fast, and highly selective RP-HPLC method was developed for the determination of Dapagliflozin (DAP) and Saxagliptin (SAX) in API and tablet dosage form. The separation was done using a Xterra RP18 (4.6×150 mm, 5 μm particle size) column with Acetonitrile: water (60:40). The isocratic elution mode at a flow rate of 1 mL/min, and the analytes were measured at 248 nm. The retention time for DAP and SAX were about 2.091 and 3.249 min, respectively. Calibration curves were found to be linear in the ranges of 100-500 μg/ml for DAP and 50-250 μg/ml for SAX, with correlation coefficients of 0.9998. The detection and quantification values for DAP was 3.0 and 9.98 μg/ml and SAX was 3.02 and 10 μg/ml respectively.
机译:开发了一种简单,快速且高度选择性的RP-HPLC方法,用于测定API和片剂剂型中的达格列净(DAP)和沙格列汀(SAX)。使用Xterra RP18(4.6×150 mm,粒径为5μm)色谱柱,用乙腈:水(60:40)进行分离。以1 mL / min的流速进行等度洗脱,并在248 nm处测量分析物。 DAP和SAX的保留时间分别约为2.091和3.249分钟。发现校正曲线在DAP 100-500μg/ ml和SAX 50-250μg/ ml范围内是线性的,相关系数为0.9998。 DAP的检测和定量值分别为3.0和9.98μg/ ml,SAX为3.02和10μg/ ml。

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